Xinyue Qi, Shouhao Zhou, Christine B Peterson, Yucai Wang, Xinying Fang, Michael L Wang, Chan Shen
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引用次数: 0

摘要

由于临床试验检测药物不良反应的能力通常不足,因此元分析是一种通过综合多项研究中与治疗相关的毒理学发现来评估药物安全性的强大工具。然而,在已发表的临床研究中经常会遇到不良事件(AEs)报告不完整的情况,尤其是当观察到的不良事件数量低于预先指定的研究阈值时。忽略通常频率较低的删减 AE 信息会使 AE 的估计发生率出现严重偏差。尽管荟萃分析中的这一普遍问题非常重要,但在文献中却很少得到统计或分析方面的关注。为了应对这一挑战,我们提出了一种贝叶斯方法,以适应安全性数据荟萃分析中的删减和可能罕见的 AE。通过模拟研究,我们证明了所提出的方法可以提高发病概率的点估计和区间估计的准确性,尤其是在存在删减数据的情况下。总之,所提出的方法提供了一种实用的解决方案,有助于在药物安全性方面做出更明智的决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meta-analysis of Censored Adverse Events.

Meta-analysis is a powerful tool for assessing drug safety by combining treatment-related toxicological findings across multiple studies, as clinical trials are typically underpowered for detecting adverse drug effects. However, incomplete reporting of adverse events (AEs) in published clinical studies is frequently encountered, especially if the observed number of AEs is below a pre-specified study-dependent threshold. Ignoring the censored AE information, often found in lower frequency, can significantly bias the estimated incidence rate of AEs. Despite its importance, this prevalent issue in meta-analysis has received little statistical or analytic attention in the literature. To address this challenge, we propose a Bayesian approach to accommodating the censored and possibly rare AEs for meta-analysis of safety data. Through simulation studies, we demonstrate that the proposed method can improve accuracy in point and interval estimation of incidence probabilities, particularly in the presence of censored data. Overall, the proposed method provides a practical solution that can facilitate better-informed decisions regarding drug safety.

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